Effect of N,C-ITO on Composite N,C-Ti/N,C-ITO/ITO Electrode Used for Photoelectrochemical Degradation of Aqueous Pollutant with Simultaneous Hydrogen Production

This study reports the effect of N,C-ITO (indium tin oxide) layer on composite N,C-TiO2/N,C-ITO/ITO (Ti/TO) electrode used for efficient photoelectrocatalytic (PEC) degradation of aqueous pollutant with simultaneous hydrogen production. The structural properties of the composite Ti/TO electrode that...

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Bibliographic Details
Main Authors: Kee-Rong Wu, Chung-Hsuang Hung, Chung-Wei Yeh, Chien-Chung Wang, Jiing-Kae Wu
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:International Journal of Photoenergy
Online Access:http://dx.doi.org/10.1155/2012/829327
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Summary:This study reports the effect of N,C-ITO (indium tin oxide) layer on composite N,C-TiO2/N,C-ITO/ITO (Ti/TO) electrode used for efficient photoelectrocatalytic (PEC) degradation of aqueous pollutant with simultaneous hydrogen production. The structural properties of the composite Ti/TO electrode that determined by X-ray diffraction and Raman scattering, show primarily the crystallized anatase TiO2 phase and distinct diffraction patterns of polycrystalline In2O3 phase. Under solar light illumination, the composite Ti/TO electrode yields simultaneously a hydrogen production rate of 12.0 μmol cm−2 h−1 and degradation rate constant of  cm−2 h−1 in organic pollutant. It implies that the overlaid N,C-TiO2 layer enhances not only the photocurrent response of the composite Ti/TO electrode at entire applied potentials, but also the flat band potential; a shift of about 0.1 V toward cathode, which is desperately beneficial in the PEC process. In light of the X-ray photoelectron spectroscopy findings, these results are attributable partly to the synergetic effect of N,C-codoping into the TiO2 and ITO lattices on their band gap narrowing and photosensitizing as well. Thus, the Ti/TO electrode can potentially serve an efficient PEC electrode for simultaneous pollutant degradation and hydrogen production.
ISSN:1110-662X
1687-529X